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Mammalian Phenotype (MP): abnormal pharynx morphology

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   respiratory system phenotype [MP:0005388] <2>(33|46) (36|29|15)
+ 1:   abnormal respiratory system morphology [MP:0002132] <12>(22|34) (27|22|13)
0:   abnormal pharynx morphology [MP:0002234] <6>(0|0) (0|0|0)
- 1:   abnormal pharyngeal muscle morphology [MP:0002253] <1>(0|0) (0|0|0)
- 1:   small pharynx [MP:0004554] <1>(0|0) (0|0|0)
- 1:   abnormal hypopharynx morphology [MP:0002250](0|0) (0|0|0)
- 1:   abnormal nasopharynx morphology [MP:0002251](0|0) (0|0|0)
- 1:   abnormal oropharynx morphology [MP:0002252](0|0) (0|0|0)
- 1:   pharynx stenosis [MP:0013174](0|0) (0|0|0)